ALKBH5 Polyclonal Antibody, 20ul Site-directed Mutagenesis Mutations in this gene have

Mutations in this gene have been associated with geroderma osteodysplastica

This gene encodes a DEAD box protein| which is a functional homolog of fission yeast Prp8 protein involved in cell cycle progression

mutations in this gene can cause autosomal recessive neuromyotonia and axonal neuropathy

Mutations in this gene are the cause of spondylometaphyseal and metatropic dysplasia and hereditary motor and sensory neuropathy type IIC

Reduced activity of this enzyme may also play a role in ataxia-telangiectasia

ALKBH5 Polyclonal Antibody, 20ul Site-directed Mutagenesis Mutations in this gene haveBelongs to the alkB family.